Sarna Whipped Foam (Hydrocortisone 1%)

Sarna Whipped Foam by

Drug Labeling and Warnings

Sarna Whipped Foam by is a Otc medication manufactured, distributed, or labeled by Crown Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SARNA WHIPPED FOAM- hydrocortisone aerosol, foam 
Crown Laboratories

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Sarna Whipped Foam (Hydrocortisone 1%)

Active Ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Uses

For the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to: eczema insect bites poison ivy poison oak poison sumac seborrheic dermatitis psoriasis other uses of this product should be only under the advice and supervision of a doctor.

Warnings

For external use only.

Contents under pressure. Do not puncture or incinerate. Avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes.

Do not use

• for external genitial, vaginal, or anal ithcing
• with other hydrocortisone product unless consulted by a doctor
• in or near the eyes
• for diaper rash

Stop use and ask a doctor if

condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Hold can at an angle and press nozzle lightly. Dispense onto hand and then apply to target area. Wipe nozzle clean after each use. Replace the overcap after each use. Children under 2 years of age: Do not use, consult a doctor.

Other Information

Store between 20° to 25°C (68° to 77°F). Do not store at temperatures above 50°C.

Inactive ingredients

Benzyl Alcohol, Carbomer, Cetyl Alcohol, Dimethicone, Glycerin, Glyceryl Stearate, Isopropyl Myristate, PEG-100, PEG-100 Stearate, Petrolatum, Propylene Glycol, Purified Water, Sodium Hydroxide, Stearic Acid

Questions?

Call 1-833-279-6522

Sarna (Hydrocortisone Foam 1%) whipped foam - 1.7 oz Canister Label

Sarna ®

Hydrocortisone Foam 1%

ECZEMA RELIEF

ANTI-ITCH

whipped foam

Fast Absorbing, Lightweight Formula

Maximum Strength Formula for Sensitive Skin

Provides fast, soothing relief from:

ECZEMA, INFLAMMATION, REDNESS, ITCH & MORE

No Parabens, Dyes or Fragrance

Net wt 1.7 oz (48 g)

Distributed by: Crown Laboratories, Inc. Johnson City, TN 37604

Sarna® is a registered trademark of Crown Laboratories, Inc.

© 2021 Crown Laboratories, Inc. sarnalotion.com

DOT 2Q M5706

P11841.00

Sarna (Hydrocortisone Foam 1%) whipped foam - 1.7 oz Carton

new

#1 DERMATOLOGIST RECOMMENDED TOPICAL, ANTI-ITCH BRAND

Sarna ®

Hydrocortisone Foam 1%

ECZEMA RELIEF

ANTI-ITCH whipped foam

Fast Absorbing, Lightweight Formula

Maximum Strength Formula for Sensitive Skin

Provides fast, soothing relief from:

ECZEMA, INFLAMMATION, REDNESS, ITCH & MORE

No Parabens, Dyes or Fragrance

Net wt 1.7 oz (48 g)

Distributed by: Crown Laboratories, Inc. Johnson City, TN 37604

Sarna® is a registered trademark of Crown Laboratories, Inc.

© 2021 Crown Laboratories, Inc.

sarnalotion.com

P11882.00

SARNA WHIPPED FOAM 
hydrocortisone aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0316-0291
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PETROLATUM (UNII: 4T6H12BN9U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARIC ACID (UNII: 4ELV7Z65AP)
CARBOMER 980 (UNII: 4Q93RCW27E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
NITROUS OXIDE (UNII: K50XQU1029)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0316-0291-17	1 in 1 CARTON	03/15/2021	10/31/2024
1		48 g in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/15/2021	10/31/2024

Labeler - Crown Laboratories (079035945)

Registrant - Crown Laboratories (079035945)

Revised: 9/2024

Document Id: 231d5e8a-f8a9-2250-e063-6394a90af7e3

34390-5

Set id: bb7436e0-6a9f-ff38-e053-2995a90a882a

Version: 5

Effective Time: 20240927